Manager, Regulatory Affairs

iRhythm Technologies, Inc. • San Francisco, CA

14d • $127,000 - $165,000 • Remote

About The Position

Career-defining. Life-changing. At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what’s possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career About This Role:

Requirements

• BA or BS degree in engineering, life sciences, or a related field required.
• > 8-10 years minimum of US and/or EU regulatory affairs experience with a Bachelor’s degree; 6 years minimum of US and/or EU regulatory affairs experience with a Master’s degree
• Demonstrated competency in operating under 21 CFR 820, EU MDD/MDR, ISO 13485, IEC 62304, ISO 14971, HIPAA and other medical device industry standards
• Software as a medical device (SaMD) experience required
• New product development experience required
• Authorship of 510(k)s and experience with management of FDA reviews to gain clearance required
• Demonstrated competency in developing risk based regulatory strategies required
• Exceptional problem-solving skills
• Exceptional organizational skills
• Exceptional communication (written and oral) skills

Nice To Haves

• Wearable medical device experience preferred
• Familiarity with global medical device regulations (LATAM, Asia Pac, EMEA, etc.) preferred
• Audit support experience preferred
• Strong project management skills
• Willingness to travel when required, approximately 5-10%

Responsibilities

• Developing and executing regulatory strategies for new and modified medical devices in line with business objectives
• Manage regulatory associates as needed, responsible for team’s work planning, guidance, execution and talent development
• Lead FDA submissions (510(k) or pre-submissions) with the team, including wearable devices, as well as artificial intelligence (AI) Software as a Medical Device (SaMD) products
• Key Regulatory SME and review & approve advertising and promotional materials to ensure regulatory compliance
• Regulatory strategy and processes for product life cycle management
• Lead EU MDR Technical Documentation and other international submissions for both wearable devices and SaMD
• Developing regulatory tools and matrices to enhance team efficiency and capabilities as needed
• Lead regulatory expert in AI, SaMD, Cybersecurity, collaborating with stakeholders establishing necessary processes to ensure regulation compliance
• Preparing international and domestic regulatory filings/registrations in line with established project timelines
• Interacting with regulatory authorities during the development and review process to ensure submission clearance
• Review and approve product design changes to maintain regulatory compliance for significant changes
• Author or revise SOPs to improve regulatory compliance within the Quality System
• Monitoring the impact of changing global regulations on submission strategies & registrations
• Support external and internal audits
• Perform other regulatory-related duties as assigned.

Benefits

• full-time position with competitive salary package and excellent benefits including medical, dental and vision insurance, paid holidays and paid time off
• iRhythm also provides additional benefits including 401K (w/ company match), an Employee Stock Purchase Plan, annual organizational/cultural committee events and more!

What This Job Offers

• Job Type: Full-time
• Career Level: Manager